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HLA dosage effect in narcolepsy with cataplexy
by
Claas, Frans H. J.
, van der Heide, Astrid
, Drabbels, Jos J. M.
, Lammers, Gert J.
, Verduijn, Willem
, Haasnoot, Geert W.
in
Alleles
/ Allergology
/ Antigens
/ Autoimmune Diseases - genetics
/ Autoimmune Diseases - immunology
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Drug dosages
/ Etiology
/ Gene Function
/ Genetic Predisposition to Disease
/ Haplotypes
/ Heterozygote
/ Histocompatibility Testing
/ HLA-DQ beta-Chains - chemistry
/ HLA-DQ beta-Chains - genetics
/ HLA-DQ beta-Chains - immunology
/ Homozygosity
/ Homozygote
/ Human Genetics
/ Humans
/ Hypothalamus
/ Immunology
/ Intracellular Signaling Peptides and Proteins - immunology
/ Intracellular Signaling Peptides and Proteins - secretion
/ Leukocytes
/ Narcolepsy - etiology
/ Narcolepsy - genetics
/ Narcolepsy - immunology
/ Neurons - immunology
/ Neurons - secretion
/ Neuropeptides - immunology
/ Neuropeptides - secretion
/ Orexins
/ Original Paper
/ Sleep disorders
2015
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HLA dosage effect in narcolepsy with cataplexy
by
Claas, Frans H. J.
, van der Heide, Astrid
, Drabbels, Jos J. M.
, Lammers, Gert J.
, Verduijn, Willem
, Haasnoot, Geert W.
in
Alleles
/ Allergology
/ Antigens
/ Autoimmune Diseases - genetics
/ Autoimmune Diseases - immunology
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Drug dosages
/ Etiology
/ Gene Function
/ Genetic Predisposition to Disease
/ Haplotypes
/ Heterozygote
/ Histocompatibility Testing
/ HLA-DQ beta-Chains - chemistry
/ HLA-DQ beta-Chains - genetics
/ HLA-DQ beta-Chains - immunology
/ Homozygosity
/ Homozygote
/ Human Genetics
/ Humans
/ Hypothalamus
/ Immunology
/ Intracellular Signaling Peptides and Proteins - immunology
/ Intracellular Signaling Peptides and Proteins - secretion
/ Leukocytes
/ Narcolepsy - etiology
/ Narcolepsy - genetics
/ Narcolepsy - immunology
/ Neurons - immunology
/ Neurons - secretion
/ Neuropeptides - immunology
/ Neuropeptides - secretion
/ Orexins
/ Original Paper
/ Sleep disorders
2015
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HLA dosage effect in narcolepsy with cataplexy
by
Claas, Frans H. J.
, van der Heide, Astrid
, Drabbels, Jos J. M.
, Lammers, Gert J.
, Verduijn, Willem
, Haasnoot, Geert W.
in
Alleles
/ Allergology
/ Antigens
/ Autoimmune Diseases - genetics
/ Autoimmune Diseases - immunology
/ Biomedical and Life Sciences
/ Biomedicine
/ Cell Biology
/ Drug dosages
/ Etiology
/ Gene Function
/ Genetic Predisposition to Disease
/ Haplotypes
/ Heterozygote
/ Histocompatibility Testing
/ HLA-DQ beta-Chains - chemistry
/ HLA-DQ beta-Chains - genetics
/ HLA-DQ beta-Chains - immunology
/ Homozygosity
/ Homozygote
/ Human Genetics
/ Humans
/ Hypothalamus
/ Immunology
/ Intracellular Signaling Peptides and Proteins - immunology
/ Intracellular Signaling Peptides and Proteins - secretion
/ Leukocytes
/ Narcolepsy - etiology
/ Narcolepsy - genetics
/ Narcolepsy - immunology
/ Neurons - immunology
/ Neurons - secretion
/ Neuropeptides - immunology
/ Neuropeptides - secretion
/ Orexins
/ Original Paper
/ Sleep disorders
2015
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Journal Article
HLA dosage effect in narcolepsy with cataplexy
2015
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Overview
Narcolepsy with cataplexy is a sleep disorder caused by the loss of hypocretin-producing neurons in the hypothalamus. It is tightly associated with a specific human leukocyte antigen (HLA)-allele:
HLA
-
DQB1
*
06
:
02
. Based on this, an autoimmune process has been hypothesized. A functional
HLA
-
DQ
molecule consists of a
DQ
α and a
DQ
β chain.
HLA
-
DQB1
*
06
:
02
(
DQ
β) has a strong preference for binding to
HLA
-
DQA1
*
01
:
02
(
DQ
α), and together they form the functional
DQ0602
dimer. A dosage effect would be expected if the
HLA
-
DQ0602
dimer itself is directly involved in the aetiology. An increased expression of the
HLA
-
DQ0602
dimer is expected in individuals homozygous for
HLA
-
DQB1
*
06
:
02
-
DQA1
*
01
:
02
, but is also hypothesized in individuals heterozygous for
HLA
-
DQB1
*
06
:
02
and homozygous for
HLA
-
DQA1
*
01
:
02
. To study the impact of the expression of the
HLA
-
DQ0602
dimer on narcolepsy susceptibility, 248 Dutch narcolepsy patients and 1272 Dutch control subjects, all of them positive for
DQB1
*
06
:
02
(heterozygous and homozygous), were HLA-genotyped with attention not only to
DQB1
but also to
DQA1
*
01
:
02. DQB1
*
06
:
02
-
DQA1
*
01
:
02
homozygosity was significantly more often seen in patients compared to controls (O.R. 2.29) confirming previous observations. More importantly, a significantly higher prevalence of homozygosity for
DQA1
*
01
:
02
was found in
HLA
-
DQB1
*
06
:
02
heterozygous patients compared to controls (O.R. 2.37,
p
< 0.001). The latter finding clearly supports a direct role of the
HLA
-
DQ
molecule in the development of disease.
Publisher
Springer Berlin Heidelberg,Springer Nature B.V
Subject
/ Antigens
/ Autoimmune Diseases - genetics
/ Autoimmune Diseases - immunology
/ Biomedical and Life Sciences
/ Etiology
/ Genetic Predisposition to Disease
/ HLA-DQ beta-Chains - chemistry
/ HLA-DQ beta-Chains - genetics
/ HLA-DQ beta-Chains - immunology
/ Humans
/ Intracellular Signaling Peptides and Proteins - immunology
/ Intracellular Signaling Peptides and Proteins - secretion
/ Orexins
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